Mouse models to evaluate the function of genes associated with allergic airway disease
PURPOSE OF REVIEWIn recent years, considerable effort has been invested in developing mouse models of allergic airway disease, as a means of evaluating the role of select genes in its pathophysiology. Here, we review the principal models used in this field, including models of allergic asthma and hy...
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Veröffentlicht in: | Current opinion in allergy and clinical immunology 2012-10, Vol.12 (5), p.467-474 |
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description | PURPOSE OF REVIEWIn recent years, considerable effort has been invested in developing mouse models of allergic airway disease, as a means of evaluating the role of select genes in its pathophysiology. Here, we review the principal models used in this field, including models of allergic asthma and hypersensitivity pneumonitis. As an example of how these models can reveal novel functional roles for genes, we review our work showing a role for the stem-cell-associated gene, Cd34. Through this example, we illustrate the genetic and immunological strategies available in the field to better understand allergic airway inflammation.
RECENT FINDINGSCD34 was found to play an important role in the development of two different models of allergic disease, that is, Th2-driven allergic asthma and Th17-driven hypersensitivity pneumonitis. Using a combination of genetically modified mice as well as cell transfers and chimeric mice, we showed that CD34 is important for the efficient trafficking of hematopoietic subsets into and out of the lung, including mast cells, eosinophils and dendritic cells.
SUMMARYThe currently available array of mutant mice and animal models of allergic disease now offers an opportunity to make profound insights into these diseases and provide preclinical models for the development of therapeutics. |
doi_str_mv | 10.1097/ACI.0b013e328357cc17 |
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RECENT FINDINGSCD34 was found to play an important role in the development of two different models of allergic disease, that is, Th2-driven allergic asthma and Th17-driven hypersensitivity pneumonitis. Using a combination of genetically modified mice as well as cell transfers and chimeric mice, we showed that CD34 is important for the efficient trafficking of hematopoietic subsets into and out of the lung, including mast cells, eosinophils and dendritic cells.
SUMMARYThe currently available array of mutant mice and animal models of allergic disease now offers an opportunity to make profound insights into these diseases and provide preclinical models for the development of therapeutics.</description><identifier>ISSN: 1528-4050</identifier><identifier>EISSN: 1473-6322</identifier><identifier>DOI: 10.1097/ACI.0b013e328357cc17</identifier><identifier>PMID: 22885889</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins, Inc</publisher><subject>Allergic diseases ; Alveolitis ; Alveolitis, Extrinsic Allergic - genetics ; Alveolitis, Extrinsic Allergic - immunology ; Alveolitis, Extrinsic Allergic - physiopathology ; Animal models ; Animals ; Antigens, CD34 - genetics ; Antigens, CD34 - immunology ; Asthma ; Asthma - genetics ; Asthma - immunology ; Asthma - physiopathology ; CD34 antigen ; Dendritic cells ; Disease Models, Animal ; Drug development ; Hemopoiesis ; Humans ; Hypersensitivity - genetics ; Hypersensitivity - immunology ; Hypersensitivity - physiopathology ; Inflammation - immunology ; Inflammation - physiopathology ; Leukocytes (eosinophilic) ; Lung ; Lung - immunology ; Mast cells ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Respiratory tract diseases ; Reviews</subject><ispartof>Current opinion in allergy and clinical immunology, 2012-10, Vol.12 (5), p.467-474</ispartof><rights>2012 Lippincott Williams & Wilkins, Inc.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3897-9b12a2796236d67f209077e9cf4db9060fe2fb873e380265bfba1203b0a6b3133</citedby><cites>FETCH-LOGICAL-c3897-9b12a2796236d67f209077e9cf4db9060fe2fb873e380265bfba1203b0a6b3133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22885889$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Laprise, C</contributor><contributor>Bouzigon, E</contributor><creatorcontrib>Blanchet, Marie-Renee</creatorcontrib><creatorcontrib>Gold, Matthew J</creatorcontrib><creatorcontrib>McNagny, Kelly M</creatorcontrib><title>Mouse models to evaluate the function of genes associated with allergic airway disease</title><title>Current opinion in allergy and clinical immunology</title><addtitle>Curr Opin Allergy Clin Immunol</addtitle><description>PURPOSE OF REVIEWIn recent years, considerable effort has been invested in developing mouse models of allergic airway disease, as a means of evaluating the role of select genes in its pathophysiology. Here, we review the principal models used in this field, including models of allergic asthma and hypersensitivity pneumonitis. As an example of how these models can reveal novel functional roles for genes, we review our work showing a role for the stem-cell-associated gene, Cd34. Through this example, we illustrate the genetic and immunological strategies available in the field to better understand allergic airway inflammation.
RECENT FINDINGSCD34 was found to play an important role in the development of two different models of allergic disease, that is, Th2-driven allergic asthma and Th17-driven hypersensitivity pneumonitis. Using a combination of genetically modified mice as well as cell transfers and chimeric mice, we showed that CD34 is important for the efficient trafficking of hematopoietic subsets into and out of the lung, including mast cells, eosinophils and dendritic cells.
SUMMARYThe currently available array of mutant mice and animal models of allergic disease now offers an opportunity to make profound insights into these diseases and provide preclinical models for the development of therapeutics.</description><subject>Allergic diseases</subject><subject>Alveolitis</subject><subject>Alveolitis, Extrinsic Allergic - genetics</subject><subject>Alveolitis, Extrinsic Allergic - immunology</subject><subject>Alveolitis, Extrinsic Allergic - physiopathology</subject><subject>Animal models</subject><subject>Animals</subject><subject>Antigens, CD34 - genetics</subject><subject>Antigens, CD34 - immunology</subject><subject>Asthma</subject><subject>Asthma - genetics</subject><subject>Asthma - immunology</subject><subject>Asthma - physiopathology</subject><subject>CD34 antigen</subject><subject>Dendritic cells</subject><subject>Disease Models, Animal</subject><subject>Drug development</subject><subject>Hemopoiesis</subject><subject>Humans</subject><subject>Hypersensitivity - genetics</subject><subject>Hypersensitivity - immunology</subject><subject>Hypersensitivity - physiopathology</subject><subject>Inflammation - immunology</subject><subject>Inflammation - physiopathology</subject><subject>Leukocytes (eosinophilic)</subject><subject>Lung</subject><subject>Lung - immunology</subject><subject>Mast cells</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Respiratory tract diseases</subject><subject>Reviews</subject><issn>1528-4050</issn><issn>1473-6322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtPHDEQhC2UiFf4Bwj5mMts2vaMH0e0AoJElEuS68j2tNkJ3jXYM6z49zjaTQ4cUE7dUn9VrSpCzhksGBj15XJ5uwAHTKDgWnTKe6YOyDFrlWik4PxD3TuumxY6OCInpfwGYNwAPyRHnGvdaW2Oya9vaS5I12nAWOiUKD7bONsJ6bRCGuaNn8a0oSnQe9xgobaU5Md6H-h2nFbUxoj5fvTUjnlrX-gwFrQFP5GPwcaCZ_t5Sn5eX_1Yfm3uvt_cLi_vGi-0UY1xjFuujORCDlIFDgaUQuNDOzgDEgLy4LSqGTVw2bngLOMgHFjpBBPilHze-T7m9DRjmfr1WDzGaDdYg_U1MJPApPwPFISSXduCrGi7Q31OpWQM_WMe1za_VKj_U35fy-_fll9lF_sPs1vj8E_0t-0K6B2wTXHCXB7ivMXcr9DGafW-9yvCNpHv</recordid><startdate>201210</startdate><enddate>201210</enddate><creator>Blanchet, Marie-Renee</creator><creator>Gold, Matthew J</creator><creator>McNagny, Kelly M</creator><general>Lippincott Williams & Wilkins, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>201210</creationdate><title>Mouse models to evaluate the function of genes associated with allergic airway disease</title><author>Blanchet, Marie-Renee ; Gold, Matthew J ; McNagny, Kelly M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3897-9b12a2796236d67f209077e9cf4db9060fe2fb873e380265bfba1203b0a6b3133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Allergic diseases</topic><topic>Alveolitis</topic><topic>Alveolitis, Extrinsic Allergic - genetics</topic><topic>Alveolitis, Extrinsic Allergic - immunology</topic><topic>Alveolitis, Extrinsic Allergic - physiopathology</topic><topic>Animal models</topic><topic>Animals</topic><topic>Antigens, CD34 - genetics</topic><topic>Antigens, CD34 - immunology</topic><topic>Asthma</topic><topic>Asthma - genetics</topic><topic>Asthma - immunology</topic><topic>Asthma - physiopathology</topic><topic>CD34 antigen</topic><topic>Dendritic cells</topic><topic>Disease Models, Animal</topic><topic>Drug development</topic><topic>Hemopoiesis</topic><topic>Humans</topic><topic>Hypersensitivity - genetics</topic><topic>Hypersensitivity - immunology</topic><topic>Hypersensitivity - physiopathology</topic><topic>Inflammation - immunology</topic><topic>Inflammation - physiopathology</topic><topic>Leukocytes (eosinophilic)</topic><topic>Lung</topic><topic>Lung - immunology</topic><topic>Mast cells</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Respiratory tract diseases</topic><topic>Reviews</topic><toplevel>online_resources</toplevel><creatorcontrib>Blanchet, Marie-Renee</creatorcontrib><creatorcontrib>Gold, Matthew J</creatorcontrib><creatorcontrib>McNagny, Kelly M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Current opinion in allergy and clinical immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blanchet, Marie-Renee</au><au>Gold, Matthew J</au><au>McNagny, Kelly M</au><au>Laprise, C</au><au>Bouzigon, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mouse models to evaluate the function of genes associated with allergic airway disease</atitle><jtitle>Current opinion in allergy and clinical immunology</jtitle><addtitle>Curr Opin Allergy Clin Immunol</addtitle><date>2012-10</date><risdate>2012</risdate><volume>12</volume><issue>5</issue><spage>467</spage><epage>474</epage><pages>467-474</pages><issn>1528-4050</issn><eissn>1473-6322</eissn><abstract>PURPOSE OF REVIEWIn recent years, considerable effort has been invested in developing mouse models of allergic airway disease, as a means of evaluating the role of select genes in its pathophysiology. Here, we review the principal models used in this field, including models of allergic asthma and hypersensitivity pneumonitis. As an example of how these models can reveal novel functional roles for genes, we review our work showing a role for the stem-cell-associated gene, Cd34. Through this example, we illustrate the genetic and immunological strategies available in the field to better understand allergic airway inflammation.
RECENT FINDINGSCD34 was found to play an important role in the development of two different models of allergic disease, that is, Th2-driven allergic asthma and Th17-driven hypersensitivity pneumonitis. Using a combination of genetically modified mice as well as cell transfers and chimeric mice, we showed that CD34 is important for the efficient trafficking of hematopoietic subsets into and out of the lung, including mast cells, eosinophils and dendritic cells.
SUMMARYThe currently available array of mutant mice and animal models of allergic disease now offers an opportunity to make profound insights into these diseases and provide preclinical models for the development of therapeutics.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>22885889</pmid><doi>10.1097/ACI.0b013e328357cc17</doi><tpages>8</tpages></addata></record> |
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subjects | Allergic diseases Alveolitis Alveolitis, Extrinsic Allergic - genetics Alveolitis, Extrinsic Allergic - immunology Alveolitis, Extrinsic Allergic - physiopathology Animal models Animals Antigens, CD34 - genetics Antigens, CD34 - immunology Asthma Asthma - genetics Asthma - immunology Asthma - physiopathology CD34 antigen Dendritic cells Disease Models, Animal Drug development Hemopoiesis Humans Hypersensitivity - genetics Hypersensitivity - immunology Hypersensitivity - physiopathology Inflammation - immunology Inflammation - physiopathology Leukocytes (eosinophilic) Lung Lung - immunology Mast cells Mice Mice, Inbred BALB C Mice, Inbred C57BL Respiratory tract diseases Reviews |
title | Mouse models to evaluate the function of genes associated with allergic airway disease |
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